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Triethylsilane → 1-Bromo-4-cyclobutylbenzene

HRID 19765
ノート
印刷プレビュー

反応式

HRID 19765 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2(O)[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.C([SiH](CC)CC)C>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 12052TriethylsilaneHCID 120954191-(4-Bromophenyl)cyclobutanol

生成物 1

HCID 571850921-Bromo-4-cyclobutylbenzene収率 66.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-78 °C

実験手順

To a solution of 1.37 g of 1-(4-bromophenyl)-cyclobutanol (6 mmol) in 15 ml DCM were added 1.15 ml of triethylsilane (7.2 mmol) and the mixture was cooled to −78° C. Then 1.15 ml of boron trifluoride diethyl etherate complex were added and the reaction mixture was warmed to −40° C. and stirred for 8 h. The reaction was then quenched by addition of 10% aqueous KHCO3 and the mixture was extracted three times with DCM. The combined extracts were washed with brine, dried with magnesium sulfate and concentrated. The remaining residue was purified by column chromatography (silica gel; cyclohexane) to give 0.84 g (66%) of 1-bromo-4-cyclobutyl-benzene as a colorless liquid. 1H NMR (CDCl3, 300 MHz): δ 1.85 (m, 1H), 1.92-2.18 (m, 3H), 2.33 (m, 2H), 3.49 (quint, J=8.5 Hz, 1H), 7.08 (d, J=8.5 Hz, 2H), 7.40 (d, J=8.5 Hz, 2H).

後処理

  1. additionThen 1.15 ml of boron trifluoride diethyl etherate complex were added
  2. temperaturethe reaction mixture was warmed to −40° C.
  3. customThe reaction was then quenched by addition of 10% aqueous KHCO3
  4. extractionthe mixture was extracted three times with DCM
  5. washThe combined extracts were washed with brine
  6. dry with materialdried with magnesium sulfate
  7. concentrationconcentrated
  8. customThe remaining residue was purified by column chromatography (silica gel; cyclohexane)

出典と根拠

ORDレコード
ord-ba5135a42a2e4327955e0f6fb22ccae0
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07745477B2

反応ノート

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